99271161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22002782-G-A

99271161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22002782-G-T

99271272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22002682-T-C

99271283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22002671-A-G

99271300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22002654-G-A

99271670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22002076-G-C

99271715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22002039-G-A

99271783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22001976-T-G

99271791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22001968-T-G

99272536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22001821-G-T

http://identifiers.org/hco/6/GRCh38#99272570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22001787-C-A

http://identifiers.org/hco/6/GRCh38#99272583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22001780-C-A

99272596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22001768-T-C

99272647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22001715-A-G

99272846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22001516-A-G

99273002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22001363-G-T

http://identifiers.org/hco/6/GRCh38#99273127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22001237-C-A

99273127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22001237-C-T

99273412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000993-G-T

http://identifiers.org/hco/6/GRCh38#99273442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22000964-C-A

99273449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000957-T-C

99273503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000917-G-T

http://identifiers.org/hco/6/GRCh38#99273529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22000891-C-A

99273642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000741-A-T

http://identifiers.org/hco/6/GRCh38#99273678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22000706-C-A

99273865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000534-A-G

99273989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000418-A-G

99274041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000368-T-G

99274184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000250-G-T

99274216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000217-G-A

99274216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000217-G-T

http://identifiers.org/hco/6/GRCh38#99274227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22000163-A-C

http://identifiers.org/hco/6/GRCh38#99274265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#22000122-C-A

99274328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000070-T-C

99274366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 22000032-A-G

99274404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21999995-T-C

99274434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21999966-T-C

99274457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21999943-C-T

99274496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21999905-A-G

99274553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21999848-A-G

99274553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21999848-A-T

99274568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21999837-G-T

http://identifiers.org/hco/6/GRCh38#99274719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21999713-A-C

99274719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21999713-A-G

99275054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21999436-G-T

99275181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21999318-G-A

99275658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21998857-C-T

99276290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21998289-T-C

99276448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21998105-G-A

99276561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21997771-T-C

99277188-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21997170-A-G

99277203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21997157-G-T

99277223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21997137-A-G

99277303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21997062-A-G

http://identifiers.org/hco/6/GRCh38#99277396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21996968-C-A

99277397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996967-T-C

99277415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996948-C-T

99277431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996932-G-A

99277431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996932-G-T

99277454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996909-G-A

99277454-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996909-G-C

99277454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996909-G-T

http://identifiers.org/hco/6/GRCh38#99277490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21996869-C-A

99277490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996869-C-T

99277621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996726-C-T

99277654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996689-G-A

99277654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996689-G-T

http://identifiers.org/hco/6/GRCh38#99277725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21996643-C-A

99277777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996603-A-G

99277861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996559-G-T

99277869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996551-C-T

http://identifiers.org/hco/6/GRCh38#99278059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21996458-C-A

http://identifiers.org/hco/6/GRCh38#99278129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21996393-C-A

99278129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21996393-C-T

99278955-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21995632-G-C

99278955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21995632-G-T

99279203-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21995427-T-A

http://identifiers.org/hco/6/GRCh38#99279451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21995196-A-C

99279491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21995161-G-T

99279552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21995103-T-C

99279555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21995097-G-A

99279555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21995097-G-T

http://identifiers.org/hco/6/GRCh38#99279610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21995052-C-A

99279731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994955-G-A

99279731-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994955-G-T

99279784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994899-G-A

99279803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994869-G-T

99279934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994770-T-G

99280186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994541-T-C

99280186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994541-T-G

http://identifiers.org/hco/6/GRCh38#99280225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21994502-C-A

99280229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994498-G-C

99280381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994373-A-G

http://identifiers.org/hco/6/GRCh38#99280523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21994234-C-A

99280523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994234-C-T

99280564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994196-A-G

99280576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994184-A-T

99280667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994092-A-G

99280676-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994083-G-A

99280696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21994063-C-T

99280781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21993966-G-A

99280781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21993966-G-T

99281034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21993714-G-C

http://identifiers.org/hco/6/GRCh38#99281056-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21993692-C-A

99281085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21993663-C-T

http://identifiers.org/hco/6/GRCh38#99281113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21993635-C-A

99281125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21993622-G-A

99281125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21993622-G-T

99281141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21993606-A-G

99281458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21993291-A-G

99281459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 21993290-G-T

99281500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21993250-T-C

99281798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992574-A-T

99281951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992443-G-A

99282006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992388-T-C

99282025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992367-G-A

99282111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21992290-C-T

99282913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990835-T-C

99283012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990759-C-G

99283012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990759-C-T

99283033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990738-T-C

99283115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990659-T-C

99283232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990556-G-A

99283327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21990469-T-C

99283890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21988058-C-G

99283938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21988004-T-C

99283992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987952-T-C

99284154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21987789-C-T

99284236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987715-T-C

99284257-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987700-T-A

99284343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987616-G-T

99284428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987518-T-C

99284473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987476-A-G

99284474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987475-G-C

99284499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987450-A-T

99284501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987448-A-G

99284510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987439-G-A

99284847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987385-G-C

http://identifiers.org/hco/6/GRCh38#99285047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21987230-C-A

99285178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987097-G-A

99285178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987097-G-C

99285231-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987057-T-C

99285282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21987015-A-G

99287704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21982702-T-C

http://identifiers.org/hco/6/GRCh38#99291647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21982549-C-A

http://identifiers.org/hco/6/GRCh38#99291659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21982541-C-A

99291659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21982541-C-G

http://identifiers.org/hco/6/GRCh38#99291660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21982540-A-C

99291890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21982334-G-A

99291892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21982332-A-G

http://identifiers.org/hco/6/GRCh38#99291955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21982279-C-A

99291955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21982279-C-G

99291955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21982279-C-T

99292006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21982232-T-C

99292125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21982120-G-C

99292288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21981960-T-C

99292296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21981952-G-A

99292426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21981824-G-A

99293300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21980279-C-T

99293387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21980212-C-T

99293469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21980117-T-C

99293638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21979930-A-G

99293716-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21979886-G-C

99294028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21979582-C-T

99294157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21979271-C-G

99294231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21979190-C-G

99294353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21978765-A-G

http://identifiers.org/hco/6/GRCh38#99294370-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21978748-A-C

99294399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21978720-C-G

99294452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21978670-A-T

99298888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21977400-T-A

99299056-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21977262-C-G

99299132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21977184-C-T

99299176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21977143-G-A

99299247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21977091-C-T

99299432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21976953-T-C

99299440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21976948-A-G

99299608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21976778-T-G

99299628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21976758-A-G

http://identifiers.org/hco/6/GRCh38#99299652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21976732-C-A

99299652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21976732-C-T

99299945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21976421-T-C

http://identifiers.org/hco/6/GRCh38#99300343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21976079-C-A

99300509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21975905-C-T

99300518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21975896-T-C

99300626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21975503-T-C

99300839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21975293-A-G

99300871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21975261-T-C

99300884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21975248-G-A

99301048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21975088-C-T

99301203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21974946-A-G

99301776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21974187-C-T

99301831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21974135-C-T

99304878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21971356-G-T

99304994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21971261-G-A

99305146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21971142-G-A

http://identifiers.org/hco/6/GRCh38#99305178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21971112-C-A

99305195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21971095-A-G

99305302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21970967-T-C

http://identifiers.org/hco/6/GRCh38#99305308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21970961-C-A

99305308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21970961-C-T

99305356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21970916-C-T

99305357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21970915-G-A

99305410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21970871-C-T

99305506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21970834-C-T

99305694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21970652-T-C

99309037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21970308-G-A

99309192-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21969727-T-A

99309308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21969591-T-C

99309398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21969519-A-G

99309616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21968745-C-T

99309626-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21968735-G-A

99309703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21968648-C-G

99309711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21968640-T-C

http://identifiers.org/hco/6/GRCh38#99309719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21968632-A-C

99309719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21968632-A-G

99309985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21968388-C-T

99310287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21967185-C-T

99310584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21966762-G-A

99310662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21966685-A-T

99310768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21966586-G-A

99314346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21964228-C-T

99315861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21962700-C-T

99315955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21962626-T-C

99315964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21962617-T-C

99316124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21962427-G-C

http://identifiers.org/hco/6/GRCh38#99316173-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21962376-A-C

99316749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21962209-T-C

99316756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21962202-A-G

99316789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21962154-A-G

99316799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21962144-C-T

99316873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21962069-C-T

99317262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21961680-A-T

http://identifiers.org/hco/6/GRCh38#99317441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21961498-C-A

99317590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21960993-T-G

99317767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21960843-G-A

99318320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21960636-T-A

99318320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21960636-T-G

99318400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21960564-A-G

99318424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21960527-T-C

99318560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21960457-T-C

99321732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21960021-G-A

99321814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21959940-C-T

99321815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21959939-G-A

99321865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21959888-T-C

http://identifiers.org/hco/6/GRCh38#99321973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21959772-C-A

99322011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21959734-G-C

99322691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21959339-T-A

99322864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21959187-A-T

http://identifiers.org/hco/6/GRCh38#99322938-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21959113-A-C

99323169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21958912-G-C

99323177-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21958904-T-G

99323191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21958890-G-C

http://identifiers.org/hco/6/GRCh38#99323231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21958849-C-A

99323298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21958796-T-C

99323298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21958796-T-G

99323452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 21958657-C-G

99323596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21958513-C-T

99323739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21958370-G-A

99323739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21958370-G-T

99323806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21958322-C-T

http://identifiers.org/hco/6/GRCh38#99323864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21958263-A-C

99325481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21957051-T-C

99325548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21956988-T-G

99325602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21956934-T-C

99325613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21956923-A-G

99325803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21956740-T-G

http://identifiers.org/hco/6/GRCh38#99326095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21956488-A-C

99326102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21956482-G-A

99326154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 21956431-G-A

99326458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21956230-T-C

99326882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21955810-C-G

99327003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21955714-A-G

99327003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21955714-A-T

99327381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21954234-T-A

99327381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21954234-T-C

99327381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21954234-T-G

99327464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21954163-T-C

99327486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21954124-T-C

99327601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21954013-T-C

99327601-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21954013-T-G

99328541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21953293-C-G

99328623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21953213-A-G

99328625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21953211-C-T

http://identifiers.org/hco/6/GRCh38#99328637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21953196-C-A

99328637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21953196-C-T

99328653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21953180-C-T

99328728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21953107-A-T

http://identifiers.org/hco/6/GRCh38#99328768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21953065-C-A

99328867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21952949-T-C

99328928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21952896-C-G

99328928-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21952896-C-T

99329502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21952115-A-G

99329634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21952004-C-T

99329771-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21951869-C-G

99330297-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21951609-A-T

99330392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21951520-G-A

99330870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21951086-G-C

99330994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21950996-A-G

99331423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21950742-G-A

99331423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21950742-G-T

99331674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21950460-A-G

99331792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21950348-G-A

http://identifiers.org/hco/6/GRCh38#99331799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21950341-A-C

http://identifiers.org/hco/6/GRCh38#99331856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21950281-A-C

99331860-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21950277-A-T

99331900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21950257-C-T

99332432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21949760-G-A

99332802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21949390-T-C

99333042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21949196-C-T

99333217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21949010-G-C

99333217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21949010-G-T

99333285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21948947-T-A

99333285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21948947-T-C

http://identifiers.org/hco/6/GRCh38#99333299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21948931-C-A

99333299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21948931-C-G

99333313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21948917-T-C

99333650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21948043-A-G

99334067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21947628-T-C

99334076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21947618-C-G

99342308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21937013-G-C

http://identifiers.org/hco/6/GRCh38#99342761-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21936889-A-C

http://identifiers.org/hco/6/GRCh38#99342789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21936861-C-A

99342789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21936861-C-G

99342825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21936824-T-C

99342825-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21936824-T-G

http://identifiers.org/hco/6/GRCh38#99342859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21936805-C-A

99342868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21936796-T-C

99342884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21936780-T-C

99343151-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21936515-G-T

99343314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21936387-T-C

99343392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21936353-A-G

99344325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21935793-C-T

99344417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21935710-C-T

99344419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21935708-A-G

99344841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21935327-T-C

99344998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21935172-G-A

99345164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21934985-G-C

99346056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21934058-T-C

99346194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21933938-G-A

99346242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21933880-C-G

99346304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21933837-C-T

99346326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21933815-T-G

99347682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21933263-T-C

99347836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21933109-T-C

99348004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21932940-G-C

99348160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21932805-G-A

99348292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21932670-C-T

99348501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21932453-A-G

99348512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21932442-A-T

99348859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21932103-C-G

99348943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21932001-C-T

http://identifiers.org/hco/6/GRCh38#99349014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21931922-C-A

99349024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21931912-G-A

99349024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21931912-G-T

99349027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21931909-A-G

99349027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21931909-A-T

99349066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21931868-C-T

99349506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21931445-G-A

99349506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21931445-G-T

99349627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21931357-G-A

99349627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 21931357-G-T

http://identifiers.org/hco/6/GRCh38#99349699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21931285-C-A

99349699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 21931285-C-T

99349753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21931231-C-T

99349870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21931162-G-A

99349870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21931162-G-T

http://identifiers.org/hco/6/GRCh38#99349901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21931148-C-A

99349901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21931148-C-T

99349944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21931111-A-G

http://identifiers.org/hco/6/GRCh38#99349946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21931109-C-A

99349946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 21931109-C-T

99350034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21931043-G-A

99350034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21931043-G-T

http://identifiers.org/hco/6/GRCh38#99350039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#21931038-C-A

99350039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21931038-C-G

99350039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20742
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 21931038-C-T